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Earlier work indicates that the cholesterol-lowering drug, simvastatin, is anabolic to chondrogenic expression of rat intervertebral disc (IVD) cells, which suggests a potential role for simvastatin in IVD regeneration. In this study, we expand on our earlier work to test the effectiveness of simvastatin on disc degeneration utilizing a rat tail disc degeneration model.
30 rats that underwent 21 G needle-puncture at rat tail discs were injected with simvastatin-loaded poly(ethylene glycol)-poly(lactic acid-co-glycolic acid)-poly(ethylene glycol) (PEG-PLGA-PEG) gel (5 mg/ml) or vehicle control at 4 weeks after needle injury. All animals were sacrificed 2 weeks after simvastatin injection. Bone morphogenetic protein-2 (BMP-2), aggrecan, collagen type II, and collagen type I messenger ribonucleic acid (mRNA) expression in the rat nucleus pulposus (NP) were measured by real-time polymerase chain reaction (PCR). In vivo magnetic resonance imaging (MRI) was performed to monitor changes in disc degeneration. Rat discs were also assessed by histology using hematoxylin and eosin (H&E) and safranin O staining. In addition, the NP weight, glycosaminoglycan (sGAG) and DNA content were also measured.
A single dose of simvastatin loaded in thermo-sensitive PEG-PLGA-PEG gel injected into the NP had the trend to increase aggrecan expression and sGAG content, and significantly increased mRNA levels of BMP-2, collagen type II, and the differentiation index (the ratio of collagen type II to collagen type I). The decreased NP weight, T2 intensity, as well as MRI index in the rat tail discs induced by needle puncture were significantly reversed after 2 weeks of simvastatin treatment. In addition, simvastatin treatment also improved histological changes induced by needle puncture.
A single injection of simvastatin loaded in PEG-PLGA-PEG gel into rat tail discs had the potential to retard or regenerate the degenerative disc.
Intervertebral disc (IVD) degeneration is the leading etiological contributor to low back pain and other disc disorders, which can cause significant socioeconomic impact. Disc degeneration often starts with cellular and biochemical changes in the nucleus pulposus (NP) and annulus fibrosus (AF), resulting in an imbalance between anabolism and catabolism of disc tissues. NP, the main constituent of the IVD, plays a major role in maintaining normal function of the IVD. As a consequence, any cellular, biological, or biochemical changes in the NP ultimately deteriorate disc function, leading to disc degeneration.
Despite its high prevalence, the current treatments for degenerative disc disease, including steroid injection [1,2], physical therapy [3,4], intradiscal electrothermal therapy [5,6] and invasive-surgical intervention, are limited to ameliorating symptoms and do not address the etiological problem . With the recent advances in recombinant therapeutic proteins [8,9] biological repair or regeneration of the degenerative IVD has been advocated. This novel treatment option appears promising, because it facilitates synthesis of matrix molecules that compose the IVD structure, and may also help prevent matrix degradation and/or cell death to detain the progression of disc degeneration.
Many growth factors, such as the bone morphogenetic protein (BMP) family (BMP-2, Osteogenic protein-1 (OP-1)/BMP-7, and Growth differentiation factor 5 (GDF-5)), transforming growth factor-β, insulin-like growth factor-1, and fibroblast growth factor have been investigated for their potential for biological repair and have been shown to elicit an anabolic effect on IVD cells [10-13]. A single injection of OP-1 [14-16] or GDF-5  into the degenerative disc has been demonstrated to be reparative to aberrant discal matrices in vivo. However, concerns still remain about these recombinant human growth factors, including undesired blood vessel ingrowth in the IVD and the need to provide supraphysiologic doses to obtain effectiveness. Moreover, the high cost of these recombinant proteins can be prohibitive.
Intriguingly, Mundy and colleagues  conducted an examination of more than 30,000 compounds to determine their effect on expression of the BMP-2 gene. The 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor statin, was the only compound that specifically increased BMP-2 mRNA in bone cells in vitro and subsequent bone formation in vivo. Our previous work initially illustrated that simvastatin stimulated endogenous BMP-2 expression in rat IVD cells cultured in vitro, which in turn promoted expression of a chondrogenic phenotype . The present study serves to further test the impact of simvastatin on the degenerative disc in a defined animal model. It has been recognized that needle puncture can induce mild and progressive disc degeneration that is suitable for testing potential treatments for degenerative disc disease [19,20]. In this study, we used a disc degeneration model developed from our previous work, which can reproduce disc degeneration in rat tails consistently with less invasive perturbation . The simvastatin-loaded compound was injected intradiscally and the effect of simvastatin on the degenerative disc was evaluated by changes in magnetic resonance imaging (MRI), gene expression, and biochemical and histological assays.
Sprague-Dawley rats (three months old) were obtained from Harlan Laboratories (Indianapolis, IN, USA) and were housed in groups of three rats per cage. As rats reach their skeletal maturity before 3 months of age, the concern of IVD remodeling due to growth can be eliminated for the selected rats at the predetermined age used in this study [22,23]. Experiments were performed in accordance with the Guide for the Care and Use of Laboratory Animals, and the experimental protocols were approved by the University Committee on the Use and Care of Animals at the University of Michigan.
The surgical procedure described previously was followed in this study . Briefly, anesthesia for all surgical procedures was achieved and maintained by inhalation of anesthetic isoflurane and the operative field was prepared in a sterile fashion. After palpation to determine the disc levels, a small skin cross-incision was made to help locate disc position for needle insertion. Co6/Co7 remained undisturbed as the control level. Fluoroscopy was used to visualize needle penetration and to ensure that the stab went into the center of the NP. A 21-gauge (G) needle was then inserted in the middle of the appropriate disc, controlled by a locking forceps clamped at 5 mm from the needle, through the AF into the NP of Co5/Co6 and Co7/Co8, rotated 180°, and held for five seconds.
Four weeks after stab injury using the 21-G needle, either poly(ethylene glycol)-poly(lactic acid-co-glycolic acid)-poly(ethylene glycol) (PEG-PLGA-PEG) gel loaded with 2 μL of simvastatin (LKT Laboratories, St. Paul, MN, USA) or gel alone was slowly injected into the NP of Co5/Co6 and Co7/Co8 randomly using a microsyringe attached to a 31-G needle. The drug-loaded compound contained simvastatin at a concentration of 5 mg/mL. The 31-G needle was chosen for drug injection based on our trial results, because it does not cause injury leading to disc degeneration. The tri-block PEG-PLGA-PEG polymer was chosen as the drug vehicle, because it has the desired properties of being thermo-sensitive, biodegradable, biocompatible, and injectable, and it has been demonstrated to extend the duration of drug exposure [24,25]. For all subsequent experiments, four experiment groups were generated: the intact control group (without needle puncture, without gel injection); the stabbed group (with needle puncture, without gel injection); the gel-alone treatment group (with needle puncture, gel only injection); and the simvastatin treatment group (with needle puncture, gel loaded with simvastatin injection). At two weeks after the injection of gel loaded with or without simvastatin, the approached caudal spine levels of rat tails were assessed.
Total RNA was extracted from the NP using the Trizol (Invitrogen, Carlsbad, CA, USA) reagent followed by RNeasy Mini Kit (Qiagen, Inc., Valencia, CA, USA). Reverse transcription was carried out at 42°C for 50 minutes using the SuperScript First-Strand Synthesis Kit (Invitrogen, Carlsbad, CA, USA). Type II collagen, type I collagen, aggrecan, BMP-2, and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) gene expression were quantified by real-time PCR using Gene Amp 7700 Sequence Detection System (Applied Biosystems, Foster City, CA, USA). A positive standard curve for each primer was obtained by real-time PCR with serially-diluted cDNA sample mixture. Quantities of gene expression of BMP-2, aggrecan, and type I and type II collagens were calculated with standard samples and normalized with GAPDH. The amounts of mRNA expression were presented as a ratio to the intact control group.
At two weeks after injection of either gel loaded with simvastatin or gel alone, the approached caudal spine levels of rat tails were assessed by MRI. Briefly, rats were anesthetized with a 2% isoflurane/oxygen mixture throughout the entire MRI examination. The animal was laid prone and the tail was straightened in a 7.0 T Varian MR scanner (183 mm horizontal bore; Varian, Inc., Palo Alto, CA, USA), and body temperature was maintained at 37°C using circulating heated air. A double-tuned volume radiofrequency coil was used to scan the tail region of the rats. Eight serial T2-weighted sagittal images covering the entire disc area were acquired using a spin-echo sequence with the following parameters: fat saturation on; repetition time/effective echo time, 3000/30 ms; field of view, 30 × 60 mm; matrix, 128 × 128; slice thickness, 0.5 mm; slice spacing, 0 mm; number of slices, eight; number of scans, 1 (total scan time 6.24 minutes).
A procedure described previously was followed to quantitatively analyze the obtained image slices using Analyze 7.0 software (AnalyzeDirect, Overland Park, KS, USA) . The nucleus region was segmented from the sliced images, followed by image reconstruction and volume rendering procedures to generate volumetric images and therefore calculate each nuclear volume. All image assessments described were conducted by three independent, blinded observers and the quantitative data were presented as the mean of the three evaluations. T2-weighted density as well as MRI index (the area of NP multiplied by average signal intensity) were quantified and calculated. For the MR index calculation, the NP area was defined by an image threshold automatically assigned by an image analysis software Analyze 7.0, which detects the default image densities over the acquired regions.
After discs were isolated from each level, a small incision was created in the AF by a sharp scissor and the entire NP (the gelatinous tissue) was taken out carefully using a micro scoop (Circon MicroSurgical, Santa Barbara, CA, USA). The dissected NP was weighed using an electronic scale, and digested with papain (125 μg/mL in sterile PBS with 5 mM cysteine. HCl and 5 mM Na2EDTA, pH 6.0) at 60°C for 24 hours. The proteoglycan, mainly sulfated glycosaminoglycan (sGAG), and the DNA contents in the digested solution were assayed using the dimethyl-methylene blue method  and Hoechst dye 33258 method , respectively.
After the animals were euthanized, three to four discs from each group were harvested for histological studies. Each disc, with 3.5 ± 0.5 mm of the adjacent vertebral bodies, was fixed in 10% neutral-buffered formalin for one week, decalcified in 22.5% formic acid and 10% sodium citrate for approximately two to three days. They were then processed for paraffin embedding and sectioning into sagittal sections (10 μm thick) using a microtome. Sections were stained with H&E and safranin O with fast-green counterstaining. Histological images were analyzed qualitatively under a light microscope (Olympus BX51; Olympus, Center Valley, PA, USA) at magnifications ranging from 4× to 100× to investigate changes in NP, AF, and endplates. The histological sections were also graded by blinded observers using the scoring standard established by Masuda and colleagues .
All data were expressed as mean ± standard error. The significance of differences among the means of data for gene expression, MRI measurement, biochemical parameters, and histological scores were analyzed using one-way analysis of variance and Fisher's least significant difference as a post hoc test. A P-value of less than 0.05 was considered statistically significant.
Figure Figure11 illustrates that BMP-2 mRNA expression in the NP among the intact control, stabbed, and gel-alone-treated groups was not significantly different. When rat discs were treated with simvastatin, BMP-2 mRNA expression was significantly increased compared with that of the intact control and stabbed groups (P < 0.05).
Groups treated with simvastatin showed an increase in mRNA expression of aggrecan although the increase did not reach significance (Figure (Figure2a).2a). However, the mRNA level of type II collagen, another key phenotypical molecule of chondrogenesis, was significantly lower in the stabbed discs when compared with the intact ones (P < 0.05). When discs were treated with gel alone, the mRNA level of type II collagen changed significantly compared with that of the stabbed discs (P < 0.05). The mRNA level of type II collagen was most elevated in discs treated with the compound loaded with simvastatin. Statistical analysis showed that collagen type II mRNA expression was significantly increased in the simvastatin-treated groups when compared with the other three groups (Figure (Figure2b;2b; P < 0.05 when compared with intact control and gel-alone-treated group, and P < 0.01 when compared with stabbed group).
The mRNA expression of type I collagen that typically reflects dedifferentiation of chondrocytes was also measured in our study. The mRNA levels of type I collagen in the stabbed disc and those treated with gel alone presented an increase at two weeks after injection. When the stabbed disc was treated with simvastatin, the mRNA level of type I collagen in this group, on the other hand, was decreased. However, post hoc comparisons indicated there was no significant difference among all experimental groups (Figure (Figure2c2c).
The ratio of type II to type I collagens is typically referred to as a 'differentiation index' of chondrocytes to demonstrate the propensity for chondrogenesis. As shown in Figure Figure2d,2d, the differentiation index in the stabbed control group was significantly decreased when compared with that of the intact control group (P < 0.05). There was no significant difference between the differentiation indices of the stabbed control and gel-treated groups. However, the index of the simvastatin-treated group was significantly higher than all other groups at time of the investigation (P < 0.01).
Representative T2-weighted, midsagittal images of the approached rat caudal disc are shown in Figure Figure3.3. At two weeks after injection, MRIs of the NP in the simvastatin-treated group showed stronger signal intensities than those in the stabbed group and the group treated with hydrogel alone (Figure (Figure3a).3a). When compared with the intact control group, the T2 density and MRI index of the stabbed group were significantly decreased (P < 0.01). T2 density in the gel-alone-treated group showed a significant decrease when compared with the stabbed group (P < 0.05). However, no significant change in MRI index was noticed between the stabbed and the gel-treated groups. In the simvastatin-treated group, the T2 signals and MRI indices in the perturbed discs were all significantly increased at two weeks after injection compared with those of the stabbed group (P < 0.05) and the gel-alone-treated group (P < 0.01; Figures Figures3b3b and and3c3c).
The weight of a NP normally decreases with progression of disc degeneration. The weight of the NP in the intact control group was 3.8 ± 0.33 mg/disc. It dropped to 1.72 ± 0.24 mg/disc in the stabbed control group, which showed a significant difference compared with intact controls (P < 0.01). No significant difference was noticed between the stabbed and the gel-alone-treated groups. After stabbed discs were treated with simvastatin, the weight of the NP significantly increased compared with the stabbed control group and gel-alone-treated group (P < 0.05; Figure Figure4a4a).
The sGAG content in the stabbed groups was lower than that in the intact control group. The difference, however, was not statistically significant between the two groups. The sGAG content in the gel-alone-treated discs decreased significantly as compared with the intact control group (P < 0.05). Treatment with simvastatin increased sGAG content in the stabbed discs; however, the increase did not reach statistical significance (Figure (Figure4b4b).
To determine whether simvastatin cell viability, the DNA content in the affected NP was measured. As shown in Figure Figure4c,4c, DNA content in the stabbed and gel-alone-treated groups was significantly decreased compared with that of the intact control (P < 0.05). Two weeks of simvastatin treatment resulted in an increase in the DNA content that had decreased due to needle puncture. Post hoc analysis did not show a significant difference between the simvastatin-treated group and gel-alone-treated group.
In the intact disc stained by H&E, the boat-shaped NP comprised at least one-half of the disc area at the midsagittal cross-section. The AF was intact and the border between the AF and the NP was clearly defined. In the stabbed group, NP area in the 21-G needle-stabbed disc decreased and became irregular, with some areas densely staining. Discs in the gel-alone-treated group still displayed features of disc degeneration to a certain extent. Conversely, the cell distribution and the extracellular matrix alignment in the 21 G-needle stabbed animals treated with simvastatin were more even and regular than those in the stab and gel-alone groups. The NP area in the intact disc stained strongly with safranin O. In the stabbed discs, the positively stained area decreased. However, the stained levels were not homogenous, as some regions stained very densely compared with surrounding vicinities. The positively stained area in the gel-alone-treated group was much smaller and weaker. When the disc was treated with simvastatin, the NP area was stained more positively than those in the gel-alone-treated group (Figure (Figure55).
Semi-quantitative histological scores were 4 ± 0 for intact control, 10 ± 1.15 for stabbed control, 11.25 ± 0.48 for gel-alone-treated group, and 7.75 ± 1.49 for simvastatin-treated group. Statistical analysis showed the histological scores of the stabbed discs in the stabbed and gel-alone-treated groups significantly increased when compared with intact control discs (P < 0.01). There was no significant difference in histological scores between the stabbed and gel-alone-treated groups. The histological score of the simvastatin-treated group, however, was significantly lower than the gel-alone-treated group (P < 0.05, Figure Figure66).
IVD degeneration is mostly characterized by changes in disc morphology and composition of the extracellular matrix, as well as loss of disc cells and water content. To achieve optimal disc repair, the ideal therapy should preserve the intact architecture of the disc tissue as much as possible, while increasing the synthesis of water-absorbing molecules, such as type II collagen and proteoglycan, to restore its 'shock-cushion' function. Most of the new biology-based strategies for disc repair are based upon these principles, including autologous cell transplantation, growth factor injection, or gene delivery. The present study provides a promising alternative that is potentially more easily translated to the clinical setting. Our results show that a single dose of simvastatin loaded in PEG-PLGA-PEG gel injected into the NP of rat discs up-regulates mRNA levels of collagen type II and the differentiation index (the ratio of type II to type I collagen). The improvements were also evident in the changes in NP weight, histological morphology, and MRI at certain significant levels.
Our previous study demonstrated that simvastatin promoted expression of a chondrogenic phenotype of rat IVD cells, mainly through the up-regulated BMP-2-mediated pathway . To determine if the stimulation of BMP-2 mRNA expression can be replicated in vivo by simvastatin, gene expression of BMP-2 in NP tissue was initially measured. The results indicated that injection of simvastatin up-regulated BMP-2 mRNA levels, thus promoting an anabolic mechanism for IVD repair. Earlier studies have also proposed a similar concept to facilitate IVD repair, although the methods involved either direct exogenous supplementation of BMP-2 [12,28,29] or endogenous up-regulation of BMP-2 with the over-expression of LIM mineralization protein-1 .
The anabolic stimulus primarily included significant increases in mRNA expression of type II collagen, and the ratio of type II to type I collagen. Previous studies indicated an increase in type I collagen and a reduction in type II collagen were present in the degenerating NP . The 'differentiation index', which is defined by the ratio of gene expression of type II to type I collagen, has become a method to track the functionality of chondrocytes (or chondrocyte-like cells in the case of NP) and can be used as a reference to measure degeneration of cartilaginous tissues .
One interesting observation from our results involved chondrogenic expression stimulated by the delivered simvastatin. When normal IVD cells were treated with simvastatin, the mRNA expression of both aggrecan and type II collagen were significantly up-regulated , whereas only the mRNA level of type II collagen in the degenerative NP increased after simvastatin treatment in the present in vivo study. Due to the changes in the notochord cells during the process of disc degeneration  and the different susceptibility to the stimuli between notochord cells and chondrocyte-like cells , the discrepancy in the responsiveness of normal and degenerative rat IVD cells to simvastatin may imply that the degree of disc degeneration and/or the cell components may affect the response of treated cells. Further studies are required to explore more details before any conclusions can be drawn.
The efficacy of simvastatin was also demonstrated by changes in sGAG content, MRI analysis, and NP weight. It should be highlighted that although the MRI and histological assays showed evidence of disc degeneration in the stabbed group, the sGAG content of this group was not significantly reduced compared with the intact control. This phenomenon has been observed in previous studies, and has been attributed to condensation of the extracellular matrix as an early response to the onset of disc degeneration [21,23,35]. In the group treated with gel alone, none of the measurements were improved. Conversely, the MRI, histological assessment, and NP weight were significantly improved in the simvastatin-treated group.
Our previous study raised the concern of decreased cell viability, despite the significant augmentation of chondrogenesis in the IVD cells by simvastatin in vitro . In the present study, a similar finding was not observed according to DNA analysis. It is likely that the use of PEG-PLGA-PEG hydrogel to deliver simvastatin minimized the likelihood of exposing cells to a transiently high concentration of the drug at the time of injection. This tri-block polymer has been used extensively as a carrier for controlled drug or gene delivery [24,36,37]. Our pilot data in a separate study also demonstrated that the release profile of simvastatin from the PEG-PLGA-PEG gel in vitro was steady and sustainable (data not shown). In addition, the polymer was chosen for its property of sol-gel phase transition, and slow degradation . After simvastatin is incorporated into the liquid gel and injected into the NP, the compound rapidly converts to the gel phase as soon as it reaches body temperature. Within the gel format, it would be expected that the exposure of simvastatin to the IVD cells can be confined to the discal core and the delivery can be sustained . The safety concern of the gel is likely to be minimal, because PEG-PLGA-PEG hydrogel has been well characterized and is currently undergoing phase I clinical trials for the treatment of breast cancer .
It should be noted that a recent study showed different results by introducing BMP-2 intradiscally for 12 weeks in a rabbit degenerative disc model. In that study, the discs treated with BMP-2 developed degenerative changes . The differing results may reflect the fact that the delivered dose and the induced concentration of BMP-2 were quite different. The direct injection of 0.1 mg of BMP-2 was supraphysiological compared with the endogenous level of BMP-2 induced by simvastatin in our study. It has been reported that a dose of 0.1 mg of BMP-2 is in the optimal range for successful posterolateral fusion in rabbits . However, for achieving cartilage repair, BMP-2 was used at lower doses (1 to 15 μg) [43-45] or by over-expression of BMP-2 using a virus vector . In our previous study, the amount of induced BMP-2 (60 to 140 pg/mL) was sufficient to promote chondrogenic expression in the IVD cells (unpublished publication). Similarly, the results of this study suggest that the concentration of induced BMP-2 by simvastatin treatment is in the therapeutic range to achieve disc repair. The degree of disc degeneration may have also resulted in the conflicting observed responses to BMP-2 stimuli. In the rabbit study by Huang and colleagues , the model used to simulate disc degeneration involved a full-thickness lesion created by blade penetration, whereas a mild and slower progression of disc degeneration occurred in the stabbed disc method used in our study. It has been shown that the BMP-2 receptor BMPRII was expressed predominantly in the AF associated with severe disc degeneration in our previous study , and the BMP-2 uptake at this site (where fibroblast-like cells reside) typically leads to osteophyte formation, because it has been shown in several studies that exogenous BMP-2 induced the BMPRII expression of ligamentous fibroblasts and, in turn, initiated endochondral ossification [47,48].
In addition to anabolism of chondrogenesis by simvastatin, there is evidence that statins can elicit anti-inflammatory actions in activated human chondrocytes , IL-1β-stimulated human chondrocytes , and experimental osteoarthritis in rabbits  by inhibiting the level of matrix metalloproteinase (MMP). For disc cells, increased MMPs have been found to promote disc degeneration [52-54]. A recent study even specified that the biochemical mediators of inflammation and tissue degradation including MMP-3, IL-1β and inducible nitric oxide synthase were significantly increased along with the disc degeneration that was induced by needle puncture . Of interest is whether simvastatin can also help suppress catabolism of chondrogenesis in degenerative disc, and thus, is the focus of our next study.
Local injection of a simvastatin-loaded PEG-PLGA-PEG compound was preliminarily found to promote autogenous chondrogenic disc repair and retard disc degeneration, which provides an alternative strategy for biological disc repair in a less expensive and easily applied method. Due to the limitation that the rat model may differ from the scheme of human disc degeneration, particularly in biomechanical functions and cellular components, future research including a long-term treatment study in this animal model as well as in a large animal model will be required to demonstrate more definitively that intradiscal injection of simvastatin would be useful for the retardation of disc degeneration.
AF: annulus fibrosus; BMP: bone morphogenetic protein; G: gauge; GAPDH: glyceraldehyde 3-phosphate dehydrogenase; H&E: hematoxylin and eosin; IL-1β: interleukin-1β; IVD: intervertebral disc; MMP: matrix metalloproteinase; MRI: magnetic resonance imaging; NP: nucleus pulpous; PBS: phosphate-buffered saline; PCR: polymerase chain reaction; PEG-PLGA-PEG: poly(ethylene glycol)-poly(lactic acid-co-glycolic acid)-poly(ethylene glycol); sGAG: glycosaminoglycan.
A provisional patent related to the content of the manuscript was disclosed in January 2008 and currently the utility patent following this disclosure has been prepared and filed. The ownership of the stated patent belongs to the University of Michigan and no kind of financial aids have been received to support the related research efforts.
HZ designed, carried out the entire study, participated in the acquisition of data, analyzed and interpreted data, and drafted the manuscript. LW participated in the acquisition and interpretation of the histological data. PJB performed the gel processing and drug preparation for injection. PP, VCY, SJH, FLM conceived the study and performed critical review and revision of the manuscript. CYL conceived the study, helped secure funding, revised the manuscript, and gave final approval of the version to be submitted. All authors read and approved the final manuscript.
The authors gratefully acknowledge funding support by National Institutes of Health grant R01 DE13608, and the Pilot Research Fund from the Department of Neurosurgery, University of Michigan. The authors would like to thank Kathy Sweet and Bonnie Nolan for their surgical assistance, Susan Yang for the histological analysis, Young Min Kwon and Cheol Moon for PEG-PLGA-PEG gel processing. The authors also thank Mrs. Holly Wagner for her assistance with manuscript preparation.